Association of specific organic matter compounds in size fractions of soils under different environmental controls

Inherent chemical recalcitrance and association of organic matter (OM) with minerals are mechanisms responsible for the long term preservation of OM in soils. The structural characteristics of OM are also believed to control specific interactions between OM and soil minerals. However, the extent of the relationship between recalcitrance and mineral protection and the specificity of these chemically driven interactions are not clearly understood at the molecular level. To measure chemical patterns of OM sequestration in sand-, silt-, clay-size and light fractions, we analyzed three soils, which mainly differed in carbon content and overlying vegetation, but have similar clay mineralogy, using biomarker analysis and nuclear magnetic resonance (NMR). Despite differences in environmental controls, long chain aliphatic compounds generally accumulated in the fine fractions of all soils. This accumulation is likely due to the strong interaction between recalcitrant forms of OM and soil minerals. For example, polymethylene and >C₂₀ organic acids accumulated in fine fractions, while lignin-derived phenols were protected from oxidation in silt-size fractions. Diffusion edited solution state ¹H NMR suggested that contributions from microbial-derived OM was greater in finer fractions, which is likely due to the accumulation of microbial-derived compounds or higher microbial activity in clay micro-sites. Our data suggest that, for these Prairie soils, the specific structure of OM and not environmental factors is responsible for long term preservation of OM in mineral fractions. Further research is necessary to understand the interplay between these preservation mechanisms such that the long term fate of OM can be further elucidated.     

Composition and origin of organic matter in surface sediments of Lake Sarbsko: A highly eutrophic and shallow coastal lake (northern Poland)

We present an organic geochemical study of surface sediments of Lake Sarbsko, a shallow coastal lake on the middle Polish Baltic coast. The aim was to provide evidence concerning the origin of the organic matter (OM) and its compositional diversity in surface deposits of this very productive, highly dynamic water body. The content and composition of the OM in the bottom sediments were investigated at 11 sampling stations throughout the lake basin. OM sources were assigned on the basis of bulk indicators [total organic carbon (TOC), total nitrogen (TN), δ¹³C_TOC and δ¹⁵N and extractable OM yield], biomarker composition of extractable OM and compound-specific C isotope signatures. The source characterization of autochthonous compounds was verified via phytoplankton analysis. The distribution of gaseous hydrocarbons in the sediments, as well as temporal changes in lake water pH, the concentration of DIC (dissolved inorganic carbon) and δ¹³C_DIC were used to trace OM decomposition.The sedimentary OM is composed mainly of well preserved phytoplankton compounds and shows minor spatial variability in composition. However, the presence of CH₄ and CO₂ in the bottom deposits provides evidence for microbial degradation of sedimentary OM. The transformation of organic compounds in surface, bottom and pore waters via oxidative processes influences carbonate equilibrium in the lake and seasonally favours precipitation or dissolution of CaCO₃.The data enhance our understanding of the relationships between the composition of sedimentary OM and environmental conditions within coastal ecosystems and shed light on the reliability of OM proxies for environmental reconstruction of coastal lakes.     

基于聚焦离子束-扫描电镜方法研究页岩有机孔三维结构

页岩中纳米级有机孔的大小直接影响页岩气含气量,其连通性亦对气体运移和开采至关重要。本文选择漆辽地区龙马溪组富有机质页岩,利用聚焦离子束-扫描电镜(FIB-SEM)在纳米尺度上(10 nm)进行有机孔结构的三维重构。研究结果表明:(1)FIB-SEM方法适用于微米级页岩的纳米(3 nm)孔隙结构特征研究。(2)蜂窝状有机孔发育均匀,孔径集中于10~200 nm,连通性较差;界面有机孔孔径集中于200~300 nm,局部连通性较好。(3)页岩总孔隙度与有机质含量成正比。研究认为,对于以有机孔为重要储集空间的页岩,有机质分布越集中,连续性越好,研究孔隙度的表征单元体尺度越小。     

东海盆地长江坳陷美人峰组烃源岩沉积环境与生烃潜力评价

利用东海盆地长江坳陷古新统美人峰组烃源岩的元素、热解、干酪根δ13C、镜质体反射率、岩石薄片、X射线衍射等资料,对长江坳陷美人峰组不同层段烃源岩进行沉积环境分析及生烃潜力评价。研究结果表明:美人峰组烃源岩的沉积环境整体表现为温暖潮湿的弱氧化淡水环境,古盐度和古气候是控制美人峰组烃源岩发育的主要环境因素。美人峰组第一段和第二段沉积时期,气候温暖潮湿,有大量陆源有机质输入,水体盐度相对较高,有机质保存条件较好,有机质丰度高,有机质类型以Ⅲ型为主,含少量II型,有机质已进入低成熟—成熟演化阶段,是美人峰组最具生烃潜力的层段;第三段和第四段沉积时期,气候相对干热,陆源碎屑及有机质输入少于第一段和第二段,水体盐度较低,不利于有机质保存,有机质丰度较低,有机质类型以Ⅲ型为主,有机质以低成熟演化阶段为主,生烃潜力不大;第五段和第六段沉积时期,气候恢复为温湿状态,有机质丰度较第三段和第四段高,有机质类型为Ⅲ型,但有机质热演化程度低,处于未熟状态,为无效烃源岩。随着埋深增加,美人峰组烃源岩的有机质成熟度变高,具有更大的生烃潜力。     

Constraining Sources of Organic Matter to Tropical Coastal Sediments: Consideration of Nontraditional End-members

Molar organic carbon to total nitrogen to organic phosphorus (OC:TN:OP) ratios are used in tandem with carbon isotopic values to constrain sources of organic matter (OM) to marine sediments in a tropical coastal embayment. Analysis of end-members specific to the study site indicates that the bulk OM pool cannot be modeled as a simple mixture of two end-members (terrestrial vs. marine OM), but rather reflects a more complex, multicomponent mixture. Mangrove, coral reef ecosystems, and bacterial biomass contribute OM to tropical coastal marine sediments that is compositionally distinct from traditional marine and terrestrial end-members and thus preclude the application of a classical two end-member mixing model of the sort that has been used traditionally in sediments from temperate environments. A survey of elemental ratios and carbon isotopic values of potential OM end-members reported in the literature, as well as depth profiles before and after whole-core incubation experiments conducted as part of this study, were used to evaluate the strength of OC:TN versus OC:OP ratios as OM source indices. Our study suggests that OC:TN ratios are a weaker indicator of OM source than OC:OP ratios, because: (1) the more restricted dynamic range of OC:TN ratios prevents clear distinction of terrestrial-from marine-derived OM, and (2) post-depositional changes in OC:TN ratios occur during diagenesis, obscuring the source signature of initially deposited OM. The fidelity of OM indices during early diagenesis underscores the importance of quantifying OP in sediments to assess sedimentary OM source.     

Geochemistry of organic matter and elements of black shale during weathering in Northern Guizhou,Southwestern China: Their mobilization and inter-connection

Different from previous studies on effect of weathering upon geochemical variation along a single weathered profile, this paper provides a new methodology validated by comparing a weathered outcrop samples and their stratigraphic counterpart un-weathered core samples in a nearby shallow borehole. This outcrop and borehole penetrated the Ordovician-Silurian Wufeng–Longmaxi shales, located in the same anticline structure in the northern part of Guizhou Province, Southern China. The mineral composition, major, trace and rare earth elements (REEs) composition and Rock-Eval parameters of outcrop and core samples were analyzed and compared. Organic matter (OM) was observed in the microscope and extracted for elements analysis. The results show that short-term weathering still has significant influence on OM, mineral and elemental composition of black shales. The elements composition shows the outcrop profile was moderately weathered. The REEs compositions do not alter much during weathering process and the REEs composition and their relative ratios still are valid for rock origin determination. The OM, mainly composed by graptolite and bitumen, even entering the highly-over thermal maturity, is still sensitive to the weathering with a systematic loss 30–50% of TOC along the outcrop profile, which suggests that the OM consumption is predominantly controlled by weathering duration and the distance from the weathering surface. In turn, OM has significant influence on the trace elements transportation behavior during weathering. Some trace elements associated with the OM such as V, Cr, Th, U, Ni and Co, change significantly in their absolute concentration during weathering, but their relative ratios do not necessarily change too much and might be still reliable proxies for paleo-environmental determination. The mobility of shale minerals during weathering is in the following order: plagioclase?>?potassium feldspar and dolomite >pyrite and OM. Short-term weathering can also result in considerable transportation of elements and significant variation of minerals content in black shale, which may pose potentially high environmental and engineering risk in the regions rich in black shale.     

未熟-低熟油生成机理的化学动力学研究及其初步应用

对树脂体、木栓质体、可溶有机质、富硫有机质、经细菌强烈改造过的有机质等各类与未熟─低熟油产出密切相关的样品及部分参照样品所进行的系统的化学动力学定量研究显示,虽然未熟─低熟油的产出和富集可能与多种不同的地质条件或因素有关,但它们的共同之处在于这些有机质较常规有机质具有明显偏低的成烃活化能。化学动力学模型的初步应用显示,这些有机质的确能在浅于常规生烃门限的地质条件下开始大量成烃,从而定量阐明了业已报道的各种地质条件下未熟─低熟油产出和富集的机理.     

Sorptive stabilization of organic matter in soils by hydrous iron oxides

Strong correlations between iron oxides (FeOx) and organic matter (OM) in soils have implied the importance of the former in stabilizing the latter. One mechanism thought to be important in this stabilization is sorption. We tested this possibility by reductively dissolving FeOx in a wide variety of soils and measuring the organic carbon (OC) that was solubilized. The OC dissolved from non-FeOx phases via anion exchange was corrected for by parallel control extractions. The resultant pool, reductively soluble OC, made up a minor amount of total soil OC in all but one of these soils, indicating that simple sorption reactions do not stabilize the bulk of soil OC in most mineral soils. OC:Fe ratios in the extracts from 2/3 of these soils were less than 0.22 (wt/wt), consistent with a sorbed state for this OC and showing that OC sorption by FeOx in these soils is limited by the amount of FeOx. The remaining soils had low pH and high OM concentrations; their higher OC:Fe ratios indicate inclusion of precipitated organo-Fe complexes in the extracts, which are likely only partially extracted by our method. The high volumetric ratios of OM to FeOx found in correlations between them from the literature are inconsistent with a dominant sorption control and point instead to stabilization to other mechanisms such as organo-Fe complexes or ternary associations among FeOx, OM and other minerals.     

Organic matter distribution in the modern sediments of the Pearl River Estuary

We determined biomarker concentrations and distributions for surface sediments from 54 sites in the Pearl River Estuary, China. We focus on a suite of four biomarker-based indicators for relative terrestrial to marine organic matter (OM) source: the branched-isoprenoid tetraether (BIT) index, the ratio of high/low molecular weight n-alcohols [(ΣC_26–34/(ΣC₁₆₊₁₈ + ΣC_26–34)], an analogous ratio for n-fatty acids and the ΣC₂₉-steroids/(ΣC₂₉-steroids + brassicasterol) ratio. All four exhibit the same terrestrial to marine transition seen in previous bulk δ¹³C studies, but with an abrupt decrease in the relative terrestrial contribution across the delta front to pro-delta transition. Concentrations of terrestrially-derived biomarkers show no systematic decrease across the transition. Instead, the decrease in the proportion of terrestrial OM is due to a decrease in the sedimentation rate and associated terrestrial OM burial across the delta toe. This suggests that diagenetic controls on the fate of terrestrial OM, such as increased biodegradation where sedimentation rate is low, are subordinate to sedimentological processes. Biomarker-derived temperature values are cooler than expected for the lower Pearl River catchment, suggesting that the dominant component of the terrestrial OM is derived from the cooler upland regions of the catchment. The dominance of input from more distal terrain with greater topographic relief is evidence for the importance of geomorphological control on terrigenous OM transport. Collectively, the results demonstrate the importance of sedimentological processes in the supply, deposition and transport of terrestrial OM.     

Can Rock-Eval pyrolysis assess the biogeochemical composition of organic matter during peatification?

Understanding the responses of soil organic carbon to an increase in global temperature is crucial to estimate potential feedbacks on global warming. In such a context, Rock-Eval pyrolysis has been recently proposed as a screening tool to investigate soil organic matter (SOM) chemistry and vulnerability. In order to test the validity of Rock-Eval as an indicator of SOM chemistry and of OM transformations, we compared classical Rock-Eval derived parameters (total organic carbon [TOC], Hydrogen Index [HI] and Oxygen Index [OI]) to Fourier infrared (FTIR) spectroscopy measured on peat sampled in two contrasting moisture conditions. The increase of TOC in the peat record depicted OM enrichment in aromatic moieties and lipids, whereas HI and OI, respectively, depicted the decomposition of carbohydrates and decarboxylation during early decay processes. Thought to be complementary to the classical parameters, other indicators based on the pyrolysis curve (S2) gave redundant or contradictory results. As an example, SOM cracking around 450 °C (namely the F3 component) was linked with carboxylic acids only in the dryer site. In the wetter one, no correlation was found between the F3 component and any FTIR absorption bands. This study underlined the current limitations of deconvolution derived parameters for the characterization of the biochemistry of OM. Finally, our work suggested that the routine use of Rock-Eval pyrolysis must be always associated with another characterization tool of OM, such as FTIR, to avoid misunderstanding.     

A GIS-based approach for detecting pollution sources and bioavailability of metals in coastal and marine sediments of Chabahar Bay,SE Iran

Chabahar Bay in SE of Iran is a shallow semi-enclosed environment affected by anthropogenic activities. In this paper, 19 sediment samples were collected and concentration of selected metals (Cu, Pb, Zn, Cd, Ni, Cr, Co, V and Fe) was determined using ICP-MS analytical method. Sediment samples from five stations were also selected for sequential extraction analysis and concentration of metals in each fraction was determined using ICP-OES. In order to investigate the environmental quality of Chabahar Bay, geographic information system (GIS) along with geochemical data, environmental indices and statistical analyses were used. Calculated contamination degree (C_d) revealed that most contaminated stations (Ch3, S1 and S3) are located SE of Chabahar Bay and contamination decreases in a NW direction. The S9 station, west of the bay, is also contaminated. High organic matter (OM) content in the sediments is most likely the result of fuel and sewage discharge from fishing vessels along with discharge of fishing leftovers. Significant correlation coefficient among OM, Fe, Cu, Pb, Zn and Cd seemingly reflects the importance of the role that OM and Fe oxy-hydroxides play in the metals mobility. The results of hierarchical cluster analysis (HCA), computed correlation coefficient and sequential extraction analysis suggest that Cu, Pb, Zn and Cd probably come from antifouling and sea vessel paints, while Ni, Cr, Co, V and Fe are most likely contributed by ophiolitic formations located north of the bay and/or deep sea sediments. Average individual contamination factors (ICFs) indicated that the highest health hazard from the bay is posed by Cu, Pb and Zn.     

The Diversity of Organic Matter in Marine Sediments and the Suspiciousness of Source Parameters: A Review

There are various types of Organic Matter (OM) in marine sediments, and it is of great significance to accurately estimate the source of them. The methods used in most researches include element ratio (C/N), stable isotopes (δ¹³C) and biomarkers (BIT), all of which are used for the whole sample as objects and calculated by end-member of terrestrial and marine source OM, respectively. However, OM is preserved in different ways, such as on its own recalcitrance or combining with inorganic minerals. Preservation differences make their respective parameter values change. After differential sedimentary by gravity or other factors,different preservation types of OM are enriched or dispersed, making some parameters distorted and even meaningless in some areas. Therefore, the parameters of OM measured by the whole sample are influenced by the source of OM and the way of deposition and preservation. Therefore, it is unreliable to use these parameters to study the source of OM without considering the way of preservation. Based on this, this paper put forward a method of particle separation to separate the sediment in different propertied and preservation types. According to the composition and characteristics of the OM at the specific grain level, the corresponding index and end-members value were used to calculate more accurate proportion of the OM. It is of profound significance to understand the production, aggregation, occurrence, migration and deposition of OM and its evolution in the entire carbon cycle.     

微生物降解蒙脱石层间吸附有机质的实验研究

近年来,国内外学者意识到,有机质在蒙脱石结构层间的吸附是有机质保存的重要机理之一,然而,目前关于微生物能否降解蒙脱石层间吸附有机质以及降解的程度等尚没有任何实验数据的支撑。本文试图通过人工合成含有层间吸附有机质的蒙脱石,利用海洋和湖泊沉积物中常见的降解有机质的微生物对其进行降解实验,据此探讨有机质的蒙脱石层间吸附在沉积物埋藏过程中对有机质保存的贡献。有机质选择半胱氨酸和甲苯,前者是生物生长所需的一种重要氨基酸,后者大量存在于土壤和沉积物中,多种细菌可以在有碳氢化合物的环境下将其降解。实验菌种选择恶臭假单胞杆菌(Pseudomonas putida)和腐败希瓦氏菌(Shewanella putrefaciens CN32)2种细菌,它们均为海洋和湖泊沉积物中的主导微生物,前者有较强的有机质降解能力,后者为铁的还原菌,厌氧代谢过程中能将蒙脱石结构中的Fe(III)还原为Fe(II)。通过上述不同菌种对蒙脱石层间吸附不同性质有机质的降解实验,结果显示,微生物对蒙脱石层间吸附的有机质的降解方式主要有分泌有机酸直接降解和破坏层间结构释放有机物从而进行降解。代表菌种假单胞菌和希瓦氏菌对半胱氨酸绿脱石及甲苯绿脱石的作用表明,微生物通过分泌有机酸的形式对蒙脱石层间吸附的有机质降解作用很有限,该结构在恒定的有氧和无氧条件下对保存有机质有利;希瓦氏菌在严格无氧条件下通过还原Fe(III)进行代谢,实验表明,无氧条件下,希瓦氏菌可以一定程度破坏矿物结构,释放并消耗有机物,因此,铁还原微生物对蒙脱石层间吸附有机质的保存有一定的影响,但由于微生物对矿物晶体结构的破坏能力有限,故其对层间吸附有机质降解的能力也有限;不同有机物对生物降解过程也有影响,这些影响取决于有机质的特性及有机质与细菌之间的相互作用。绿脱石层间吸附的半胱氨酸对生物生长有利,从而可能促进生物还原Fe(III)作用。相反,甲苯却很明显的抑制了Fe(III)的还原。由此可见,有机质的蒙脱石层间吸附是有机质保存的重要方式之一。     

海洋沉积物中有机质早期成岩矿化路径及其相对贡献

陆架边缘海沉积物是重要的生物地球化学反应器,海洋中90%以上的有机质沉积于此并在早期成岩作用过程中矿化.其矿化路径包括有氧呼吸、反硝化、锰氧化物还原、铁氧化物还原、SO4(-2)还原和CO2还原,并按生成自由能减少的顺序依次发生,构成理想的氧化还原序列.定量研究有机碳矿化路径及其对有机质矿化的相对贡献对揭示能量分配和碳...     

Organic matter preservation in the carbonate matrix of a recent microbial mat – Is there a ‘mat seal effect’?

Phototrophic mats (microbial mats with a phototrophic top layer) are complex systems in terms of microbial diversity, biogeochemical cycles and organic matter (OM) turnover. It has been proposed that these mats were a predominant life form in Proterozoic shallow water settings, prior to the emergence of bioturbating organisms in the Ediacaran–Cambrian transition. For most of the Precambrian, microbial mats were not only quantitative important carbon fixing systems, but also influenced the transfer and transformation of OM before it entered the geosphere. The profound alteration of compound inventories during transit through microbial mats, implying substantial consequences for OM preservation in the Proterozoic, was recently proposed as a “mat-seal effect” [Pawlowska et al. (2012) Geology 41, 103–106]. To obtain a better understanding of the early diagenetic fate of primary produced OM in microbial mats, we studied a recent calcifying mat from a hypersaline lake in Kiritimati, which showed in the deeper mat layers a maximum ¹⁴C_carbonate age of ∼1500 years. We particularly focused on OM entrapped in the carbonate matrix, because of the better potential of such biomineral-encapsulated OM to reach the geosphere before degradation (and remineralization). Our data indicate that selective preservation is important in phototrophic mats. While a diagenetic transformation of lipid fatty acids (FAs) was evident, their fatty acyl-derived hydrocarbon moieties were not introduced into protokerogen, which was instead mainly comprised of cyanobacterial and/or algal biomacromolecules. Our data support the proposed major impact of the “mat-seal effect” on OM turnover and preservation; i.e. the suppression of biosignatures derived from the upper mat layers, while signals of heterotrophic microbes thriving in deeper mat layers become preferentially preserved (e.g. high hopane/sterane ratios). This mechanism may have broad consequences for the interpretation of biomarkers from Proterozoic shelf environments, because biosignatures of phototrophic mat dwellers as well as planktonic signals may have become heavily biased by the production and turnover of OM in microbial mat systems.     

Protection of organic carbon in soil microaggregates via restructuring of aggregate porosity and filling of pores with accumulating organic matter

We examined relationships between the pore structure of microaggregates and the protection of organic matter (OM) within that structure. By using ultra-small angle X-ray scattering (USAXS) before and after combustion of microaggregates at 350 °C, we took advantage of differences in X-ray scattering contrast among soil minerals, OM, and air to evaluate the distribution of the total- and OM-filled porosity within microaggregates (53-250 μm in diameter). Systematic changes in microaggregate structure were observed for long-term field manipulations of land use (a chronosequence of tallgrass prairie restorations) and agricultural management (conventional tillage versus no-till at two levels of nitrogen fertilization). Our results imply that OM preservation arose from the evolution of the architectural system of microaggregates during their formation and stabilization. Soils and treatments with increasing OM in microaggregates were associated with encapsulation of colloidal OM by minerals, thereby creating protected OM-filled pores at the submicron scale within the microaggregate structure. For example, in the prairie chronosequence, microaggregates from the cultivated soil had the lowest concentration of OM, but 75% of the OM that had survived cultivation was in OM-filled pores. Following restoration, the concentration of OM in microaggregates increased rapidly, but the proportion of OM in OM-filled pores declined initially and then increased over time until 90% of the OM was in OM-filled pores. OM totally encapsulated within the pore structure can create spatial and kinetic constraints on microbial access to and degradation of OM. Encapsulation of OM increases the capacity for its protection relative to sorption on mineral surfaces, and comparison of its extent among treatments suggests important feedback loops. The use of USAXS, which has not previously been applied to the study of soil aggregate structures and the distribution of OM within those structures, provided new information on the mechanisms of OM protection in soil microaggregates, and insights relevant to strategies for enhancing carbon-sequestration in soil through changes in agricultural management practices and land use.     

Organic Matter Accumulation in the Upper Permian Dalong Formation from the Lower Yangtze Region, South China

The Late Permian was marked by a series of important geological events and widespread organic-rich black shale depositions, acting as important unconventional hydrocarbon source rocks. However, the mechanism of organic matter (OM) enrichment throughout this period is still controversial. Based on geochemical data, the marine redox conditions, paleogeographic and hydrographic environment, primary productivity, volcanism, and terrigenous input during the Late Permian in the Lower Yangtze region have been studied from the Putaoling section, Chaohu, to provide new insights into OM accumulation. Five Phases are distinguished based on the TOC and environmental variations. In Phase I, anoxic conditions driven by water restriction enhanced OM preservation. In Phase II, euxinic and cycling hydrological environments were the two most substantial controlling factors for the massive OM deposition. During Phase III, intensified terrestrial input potentially diluted the OM in sediment and the presence of oxygen in bottom water weakened the preservation condition. Phase IV was characterized by a relatively higher abundance of mercury (Hg) and TOC (peak at 16.98 wt%), indicating that enhanced volcanism potentially stimulated higher productivity and a euxinic environment. In Phase V, extremely lean OM was preserved as a result of terrestrial dilutions and decreasing primary productivity. Phases I, II and IV are characterized as the most prominent OM-rich zones due to the effective interactions of the controlling factors, namely paleogeographic, hydrographic environment, volcanism, and redox conditions.     

Hopane,sterane and n-alkane distributions in shallow sediments hosting high arsenic groundwaters in Cambodia

The presence of elevated As in ground waters exploited for drinking water and irrigation in South-East Asia is causing serious impacts on human health. A key mechanism that causes the mobilization of As in these waters is microbially mediated reductive transformation of As-bearing Fe(III) hydrated oxides and the role of degradable organic matter (OM) in this process is widely recognized. A number of different types of OM that drive As release in these aquifers have been suggested, including petroleum derived hydrocarbons naturally seeping into shallow sediments from deeper thermally mature source rocks. However, the amount of information on the characteristics of the OM in South-East Asian aquifers is limited. Here the organic geochemical analyses of the saturated hydrocarbon fractions and radiocarbon analysis, of two additional sites in SE Asia are reported. The results show that the OM in a given sedimentary horizon likely derives from multiple sources including naturally occurring petroleum. The importance of naturally occurring petroleum as one of the sources was clearly indicated by the n-alkane CPI of approximately 1, the presence of an unresolved complex mixture, and hopane (dominated by 17α(H),21β(H) hopanes) and sterane distribution patterns. The results also indicate that the OM in these aquifers varies tremendously in content, character and potential bioavailability. Furthermore, the presence of petroleum derived OM in sediments at both sites doubles the number of locations where their presence has been observed in association with As-rich, shallow aquifers, suggesting that the role of petroleum derived OM in microbially mediated As release might occur over a wider range of geographical locations than previously thought.     

土壤和沉积物中NOM稳定性矿物学机制研究的理论与方法

土壤和沉积物中天然有机质(NOM)稳定性问题受到关注,主要是因为NOM的稳定性直接影响到大气中CO2的平衡与全球气候变化。此外,天然有机质还影响着土壤和沉积物中矿物的表面反应性、污染物的环境行为与生物有效性。因此,本综述在详细介绍土壤和沉积物中NOM稳定性矿物学机制研究的理论与方法的同时,也简略介绍了NOM的组成结构与反应性,并着重强调NOM/矿物微界面过程作用机制的重要性。许多研究表明,土壤和沉积物中NOM稳定性的矿物学机制主要包括矿物表面吸附和物理包裹。本综述目的是,介绍矿物保护的稳定NOM的分离、特性及其分析测定方法与技术,并且强调NOM稳定性矿物学保护机制系统性研究的重要性,以搞清矿物学保护机制在土壤和沉积物中NOM稳定保持中的贡献与重要性以及矿物学保护机制对天然有机质稳定性的调控作用,从而提高对土壤和沉积物环境生态的地球化学、矿物学的认识水平。